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DePuy Mitek, Inc., a Johnson & Johnson Co. FDA Recalls
7 recalls on file across devices, 0 of them Class I and 7 still open. This firm is not matched to a listed company.
Newest first
Class I is the FDA's most serious grade: a reasonable probability of serious harm or death.
| Product |
|---|
| COR Disposable Kit, 8 mm. Cartilage Transplant System.Class IIFeb 24, 2025Device is missing the pin in the graft loader component. |
| COR Disposable Kit, 8 mm w/ Perpendicularity. Cartilage Transplant System.Class IIFeb 24, 2025Device is missing the pin in the graft loader component. |
| DePuy Mitek BIOKNOTLESS Plus w/ OC-Indicated for use in soft tissue to bone fixation in association with adequate postopClass IIApr 13, 2023IFU Warning: Applying bending force and/or bending force wit |
| DePuy Mitek BIOKNOTLESS Plus w/ Panacryl-Indicated for use in soft tissue to bone fixation in association with adequate Class IIApr 13, 2023IFU Warning: Applying bending force and/or bending force wit |
| DePuy Mitek BIOKNOTLESS Rapid w/ Pan-Indicated for use in soft tissue to bone fixation in association with adequate postClass IIApr 13, 2023IFU Warning: Applying bending force and/or bending force wit |
| DePuy Mitek BIOKNOTLESS Plus w/ Ethibond-Iindicated for use in soft tissue to bone fixation in association with adequateClass IIApr 13, 2023IFU Warning: Applying bending force and/or bending force wit |
| DePuy Mitek BIOKNOTLESS Rapid W/ OC-Indicated for use in soft tissue to bone fixation in association with adequate postoClass IIApr 13, 2023IFU Warning: Applying bending force and/or bending force wit |